HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446958Generated: October 25, 2026
2,3-Butanediol → N-(4,5-Dimethyl-1,3-dioxolan-2-YL)-N-methyl-2-chloroacetamide
https://huagongshe.com/reaction/1446958
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,3-Butanediol | HCID 262 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamide | HCID 12850700 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(4,5-Dimethyl-1,3-dioxolan-2-YL)-N-methyl-2-chloroacetamide | HCID 20551717 | — |
Reaction Steps
N-(2,2-Dimethoxyethyl)-N-methyl-2-chloroacetamide (97.8 grams; 0.5 mole), 2,3-butanediol (45 grams) and 0.2 grams p-toluenesulfonic acid were charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, distilling head and condenser. The reaction mixture was heated at about 90° C. to 100° for a period of 5 hours. Little reaction occurred as shown by the absence of methanol distilled. The reaction mixture was then heated at about 110° C., for about 2 hours at atmospheric pressure, then 1 hour at reduced pressure. Under these more rigorous conditions, methanol was formed and was distilled off. At the conclusion of the reaction, the reaction mixture was distilled and the fraction boiling at 127° C. to 130° C. at 0.55 mm Hg was the desired product N-(4,5-dimethyl-1,3-dioxolan-2-yl)-N-methyl-2-chloroacetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04314840 |
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| Source dataset | uspto-grants-1982_02 |
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| ORD ID | ord-df5f30e24d8848b2aa8a27dab98251d0 |
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| Source note | uspto-grants-1982_02 |
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